The Recall Desk

Archive

July 2025 recalls

632 recalls were announced in July 2025.

What the numbers show

Critical
4
Severe
232
High
244
Moderate
144
Low
8

Of the 632 recalls this month scored against our rubric, 1% are Critical, 37% are Severe.

101–200 of 632

  • HighNHTSA·25V483000·2025-07-24

    2026 Cadillac VISTIQ High-Voltage Battery Bolt Defect Recall

    General Motors is recalling certain 2026 Cadillac VISTIQ and 2025 Cadillac LYRIQ vehicles because bolts attaching the high-voltage battery to the floor may be missing or loose, creating a fire risk in a crash.

    Product
    CADILLAC — CADILLAC VISTIQ, LYRIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25401·2025-07-24

    LIVACTI retractable safety gates leave a gap a child can pass

    LIVACTI retractable mesh safety gates, model LT-BG01-3, are being recalled because a child's torso can fit through the opening between the gate and the floor. About 1,400 units are affected.

    Product
    LIVACTI Retractable Safety Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25404·2025-07-24

    Minecraft light-up slap bracelets allow children to access button cell batteries

    Minecraft Light-Up Slap Ruler Bracelets are being recalled because the battery compartment can be opened easily by children, violating the mandatory toy standard. About 75,900 units affected.

    Product
    Minecraft Light-Up Slap Ruler Bracelets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25399·2025-07-24

    Creekwood Naturals turpentine bottles lack the required child-resistant packaging

    Creekwood Naturals Gum Spirits of Turpentine bottles are being recalled because they violate the mandatory standard for child-resistant packaging. About 9,000 units are affected.

    Product
    100% Natural Pure Gum Spirits of Turpentine Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0270-2025·2025-07-23

    Roasted brussels sprouts recalled over potential Listeria monocytogenes contamination

    Roasted brussels sprouts packed seven 2 lb polybags per case are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 71 cases are affected.

    Product
    FG21004 Brussels Sprouts, Roasted 2514111 FG21004 Brussels Sprouts, Roasted 2514311 Packaged 7- 2 lb polybags per cardboard case
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2095-2025·2025-07-23

    Baxter SIGMA Spectrum V6 infusion pumps may carry incorrect software version

    Baxter SIGMA Spectrum Infusion Pump V6 units are being recalled because certain pumps may have an incorrect version of software. 14 units are affected.

    Product
    Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Food)·H-0265-2025·2025-07-23

    Chopped red bell peppers recalled over potential Listeria monocytogenes contamination

    Chopped red bell peppers packed in polybags and cardboard cases are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 31 cases are affected.

    Product
    FG20007 Pepper, Red Bell Chop packaged in poly bag, and cardboard case. 17.5 lbs per case
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0261-2025·2025-07-23

    Enoki mushrooms may be contaminated with Listeria monocytogenes

    Enoki Mushrooms in 200 g green and clear plastic packages are being recalled because the product may be contaminated with Listeria monocytogenes. 90 boxes are affected.

    Product
    Enoki Mushroom in a 200g, green and clear plastic package marked with UPC Barcode 6 976532 310051 on the back label; a picture of enoki mushrooms is outlined in green on the front of the package
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·H-0262-2025·2025-07-23

    Shredded red cabbage recalled over potential Listeria monocytogenes contamination

    Shredded red cabbage packed in polybags and cardboard cases is being recalled because it has the potential to be contaminated with Listeria monocytogenes. One 14 lb case is affected.

    Product
    Red cabbage, shredded packed in polybag and cardboard case. 14 lbs per case.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0267-2025·2025-07-23

    Grape tomatoes recalled over potential Listeria monocytogenes contamination

    Grape tomatoes packed four 2.5 lb polybags per case are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 141 cases are affected.

    Product
    FG20044 Tomato, Grape CV 2514111 ; 2514111B FG20004 Tomato, Grape CV 2514211 Packaged 4- 2.5lb polybags per cardboard case
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0269-2025·2025-07-23

    Cooked breakfast potatoes recalled over potential Listeria monocytogenes contamination

    Cooked breakfast potatoes packed three 5 lb polybags per case are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 98 cases are affected.

    Product
    FG21002 Potato, Cooked Breakfast 2514111; 2514111B FG21002 Potato, Cooked Breakfast 2514311 Packaged 3- 5 lb polybags per cardboard case
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·25V479000·2025-07-23

    Ferrari Purosangue fuse box contact can decrease braking ability

    Ferrari is recalling certain 2023-2025 Purosangue vehicles because the fuse box power supply and passenger-side footrest may contact each other, causing a short circuit that decreases braking ability.

    Product
    FERRARI — FERRARI PUROSANGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V481000·2025-07-23

    Tiffin motorhome alternator programming error can stall the engine

    Tiffin is recalling certain 2023-2026 motorhomes with 2.0 litre engines because the secondary alternator controller programming was not properly updated, which can stall the engine.

    Product
    TIFFIN — TIFFIN GT1, GH2, CONVOY, GH1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0281-2025·2025-07-23

    Kilwin's mocha truffles recalled over undeclared pecans in the product

    Kilwin's Mocha Truffles, in 2.5 lb bulk and 4.75 oz retail units, are being recalled because of undeclared pecans. 130 lbs in total are affected.

    Product
    Kilwin's Mocha Truffle bulk 2.5lbs Kilwin's Mocha Truffles 4.75oz UPC 0 043110 5
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Food)·H-0268-2025·2025-07-23

    Cooked breakfast potatoes in 4 lb bags recalled over Listeria risk

    Cooked breakfast potatoes packed seven 4 lb polybags per case are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 106 cases are affected.

    Product
    FG21002 Potato, Cooked Breakfast 2514111; 2514111B FG21002 Potato, Cooked Breakfast 2514311 Packaged 7- 4 lb polybags per cardboard case
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0283-2025·2025-07-23

    Kilwin's family assortments recalled over undeclared pecans in the product

    Kilwin's Family Assortment in 9 oz, 14 oz, 28 oz and 42 oz sizes is being recalled because of undeclared pecans. 130 lbs in total are affected.

    Product
    Kilwin's Family Assortment 9oz UPC 0 004564 3 Kilwin's Family Assortment 14oz UPC 0 004565 0 Kilwin's Family Assortment 28oz UPC 0 004566 7 Kilwin's Family Assortment 42oz UPC 0 004567 4
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Devices)·Z-2102-2025·2025-07-23

    i-view video laryngoscopes may be faulty because of depleted batteries

    The i-view video laryngoscope is being recalled because of the potential for faulty devices as a result of depleted batteries. 2,152 pieces are affected.

    Product
    i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.
    Category
    Medical Device
    Distribution
    17 states
  • SevereFDA (Food)·H-0282-2025·2025-07-23

    Kilwin's truffle assortments recalled over undeclared pecans in the product

    Kilwin's Truffle Assortments in 9.5 oz, 8 oz and 4.75 oz sizes are being recalled because of undeclared pecans. 130 lbs in total are affected.

    Product
    Kilwin's Truffle Assortment 9.5oz UPC 0 004574 0 Kilwin's Truffle Assortment 8oz UPC 0 043109 5 Kilwin's Truffle Assortment 4.75oz UPC 0 044121 8
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Food)·H-0264-2025·2025-07-23

    Sliced cucumbers recalled over potential Listeria monocytogenes contamination

    Sliced cucumbers packed in polybags and cardboard cases are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 8 cases are affected.

    Product
    FG20004 Cucumber, Sliced packaged in poly bag, and cardboard case. 16 lbs per case
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0318-2025·2025-07-23

    Aunt Mid's fresh sliced mushrooms recalled over potential Listeria contamination

    Aunt Mid's Fresh Sliced Mushrooms in 8 oz packages are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 175 cases are affected.

    Product
    Aunt Mid's Fresh Sliced Mushrooms 227g (8 oz.) BEST BEFORE 25JL04 MEILLEUR AVANT, UPC 0 33383 676005 on top and best before date of BEST BEFORE 25JL04 stamped on side, 12 packages per case
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·H-0316-2025·2025-07-23

    Peeters Mushroom Farm cremini sliced mushrooms recalled over potential Listeria contamination

    Peeters Mushroom Farm Cremini Sliced Mushrooms in 8 oz packages are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 25 cases are affected.

    Product
    Peeters Mushroom Farm Cremini Sliced mushrooms 227g (8 oz.) UPC 0 68414 96960 3, flat black plastic package, BEST BEFORE 25JL04 stamped on side, 12 packages per case
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2096-2025·2025-07-23

    Baxter SIGMA Spectrum V8 infusion pumps may carry incorrect software version

    Baxter SIGMA Spectrum Infusion Pump V8 units are being recalled because certain pumps may have an incorrect version of software. 28 units are affected.

    Product
    Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Food)·H-0263-2025·2025-07-23

    Diced red onions recalled over potential Listeria monocytogenes contamination

    Diced red onions packed in polybags and cardboard cases are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 8 cases are affected.

    Product
    FG20001 Onion, Red Diced packaged in poly bag and cardboard case. 18 lbs per case
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0266-2025·2025-07-23

    Shredded carrots recalled over potential Listeria monocytogenes contamination

    Shredded carrots packed 12 polybags per case are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 195 bags across 16 cases are affected.

    Product
    FG20009 Carrot, Shred; 12 poly bags per cardboard case; 18 lbs per case
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0305-2025·2025-07-23

    Dubai emek pistachio cacao spread may be contaminated with Salmonella

    Dubai emek Spread Pistachio Cacao Cream with Kadayif is being recalled after the FDA notified the firm that the product may be contaminated with Salmonella. 316 cases are affected.

    Product
    Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. 9.7oz UPC 8 69652 10130 1 Manufacturer: Emek Dogal Saglik Urunlerilkl. Gida Turkey
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·H-0306-2025·2025-07-23

    Danshi shredded tofu recalled because sesame is not declared on label

    Danshi branded Shredded Tofu 200g is being recalled because the product does not declare the allergen ingredient sesame. 50 cases are affected.

    Product
    Front Panel: Danshi branded Shredded Tofu, 200g Rear Panel: Best before: 05/24/2025, Imported by: Shang Hao Jia, Inc. Address: South El Monte, CA 91733. Product of China. Manufacturer: Sichuan Shifang Danshi Food Co., Ltd. UPC: 6 942849 709499
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0317-2025·2025-07-23

    Peeters Mushroom Farm thick sliced mushrooms recalled over potential Listeria contamination

    Peeters Mushroom Farm Thick Slice Mushrooms in 10 lb containers are being recalled because they have the potential to be contaminated with Listeria monocytogenes. 10 cases are affected.

    Product
    Peeters Mushroom Farm Thick Slice Mushroom 10lb cardboard container labeled with Peeters Mushroom Farm
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·H-0271-2025·2025-07-23

    Seal the Seasons frozen organic blueberries contaminated with Listeria monocytogenes

    Seal the Seasons Frozen Organic Blueberries are being recalled after the firm was notified by its supplier that the product is contaminated with Listeria monocytogenes. 208 cases are affected.

    Product
    SEAL THE SEASONS FROZEN ORGANIC***BLUEBERRIES NET WT. 32 OZ (907g) NC UPC 8 50476 00647 1; NJ UPC 8 50037 94831 ? DISTRIBUTED BY: Seal the Seasons Inc. 4426 S. Miami Blvd. Durham, NC 27703
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·25V395000·2025-07-23

    BMW electric drive motor software can shut down high voltage system

    BMW is recalling certain 2022-2025 i4, 2022-2024 iX, 2023-2024 i7 and 2024 i5 vehicles because electric drive motor software may shut down the high-voltage system, causing a loss of drive power.

    Product
    BMW — BMW I5, IX, I4, I7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2112-2025·2025-07-23

    BLS laser show projectors shipped without a working remote interlock connector

    BLS laser light show projectors, models CLUB 1000, 2000 and 4000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 12 units affected.

    Product
    Laser light show projectors manufactured by BLS, Model CLUB 1000/2000/4000.
    Category
    Other
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2126-2025·2025-07-23

    EMPOWR 3D knee tibial inserts were packaged with the wrong implant

    EMPOWR 3D Knee Tibial Insert E-PLUS units are being recalled because of a packaging discrepancy in which incorrect tibial inserts were packaged. 20 units are affected.

    Product
    Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11L 12MM, VE Model/Catalog Number: 341-12-711 Software Version: NA Product Description: Enovis" knee devices are intended for treatment of patients who are candidates for knee arthroplasty p
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Drugs)·D-0532-2025·2025-07-23

    Lisinopril and hydrochlorothiazide bottle contained a foreign antiretroviral tablet

    Lisinopril and Hydrochlorothiazide Tablets 20 mg/12.5 mg are being recalled after a complaint that a sealed bottle contained a foreign tablet identified as atazanavir and ritonavir. 58,968 bottles affected.

    Product
    LISINOPRIL AND HYDROCHLOROTHIAZIDE — LISINOPRIL AND HYDROCHLOROTHIAZIDE (LISINOPRIL AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0302-2025·2025-07-23

    YoCrunch strawberry two-product yogurt packages may contain plastic pieces

    YoCrunch Lowfat Yogurt with Toppers two-product packages containing strawberry yogurt with M&Ms and with Oreo pieces are being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Lowfat Yogurt with Toppers. Two-product package. Contains 8-6oz (170g) cups of Strawberry Yogurt with milk chocolate M&Ms pieces (cup UPC 46675-00084), and 8-6oz (170g) cups of Strawberry Yogurt with Oreo pieces (cup UPC46675-00083). Two-Pack UPC 46675-02613. Kee
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0290-2025·2025-07-23

    Cotton Candy Twirl bars recalled over potential Listeria monocytogenes contamination

    Cotton Candy Twirl Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Cotton Candy Twirl Bar (86260), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighNHTSA·25V482000·2025-07-23

    Hyundai IONIQ 5 battery bus bar may be improperly tightened

    Hyundai is recalling certain 2025 IONIQ 5 vehicles because the high voltage battery may contain an improperly tightened bus bar that can short circuit. Owners are told to park outside until repaired.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2121-2025·2025-07-23

    VITROS Performance Verifier II lots can cause quality control drift

    VITROS Chemistry Products Performance Verifier II is being recalled because quality control drift can occur with certain cholinesterase slide lots, which could produce erroneous patient results.

    Product
    Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products Performance Verifier II Model/Catalog Number: 8231474 Software Version: N/A Product Description: VITROS Chemistry Products Performance Verifier is an assayed control used to monitor performance on V
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2123-2025·2025-07-23

    VITROS CHE slides sold in Japan can cause quality control drift

    VITROS Chemistry Products CHE Slides supplied in Japan are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.

    Product
    VITROS Chemistry Products CHE Slides (Japan); Catalog Numbers: (1) 684 4074 (90 slides), (2) 684 4138 (300 slides);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0287-2025·2025-07-23

    Crumbled cookie bars recalled over potential Listeria monocytogenes contamination

    Crumbled Cookie Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Crumbled Cookie Bar (85200), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·H-0292-2025·2025-07-23

    Savagely Sour cherry bars recalled over potential Listeria monocytogenes contamination

    Savagely Sour Cherry Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Savagely Sour Cherry Bar (86266), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Drugs)·D-0522-2025·2025-07-23

    Levothyroxine sodium 112 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 112 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 4,896 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0523-2025·2025-07-23

    Levothyroxine sodium 150 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 150 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 4,921 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0301-2025·2025-07-23

    YoCrunch vanilla two-product yogurt packages may contain plastic pieces

    YoCrunch Lowfat Yogurt with Toppers two-product packages containing vanilla yogurt with M&Ms and with Oreo pieces are being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Lowfat Yogurt with Toppers. Two-product packages. 1. Contains 8- 6oz (170g) cups of Vanilla Yogurt with milk chocolate M&Ms pieces (cup UPC 46675-00079), and 8-6oz (170g) cups of Vanilla Yogurt with Oreo pieces (cup UPC 46675-00080). Two-pack UPC 46675-01400.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0289-2025·2025-07-23

    Fudge Frenzy bars recalled over potential Listeria monocytogenes contamination

    Fudge Frenzy Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Fudge Frenzy Bar (86210), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·H-0295-2025·2025-07-23

    YoCrunch vanilla yogurt with Oreo pieces may contain plastic material

    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Oreo cookie pieces, is being recalled because of foreign material in the form of plastic.

    Product
    YoCrunch Low Fat Yogurt with toppers. Vanilla with Oreo cookie pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00080 2. Multipack containing 4-4 oz. cups UPC 46675-01350 Keep Refrigerated. Distributed by Danone US, LLC, White
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0286-2025·2025-07-23

    Rich Bar frozen novelties recalled over potential Listeria monocytogenes contamination

    Rich Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Rich Bar (85155), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·H-0285-2025·2025-07-23

    Strawberry Shortcake bars recalled over potential Listeria monocytogenes contamination

    Strawberry Shortcake Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Strawberry Shortcake Bar (85050), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·H-0303-2025·2025-07-23

    YoCrunch Snickers and Twix yogurt packages may contain plastic pieces

    YoCrunch Lowfat Yogurt with Toppers two-product packages containing vanilla yogurt with Snickers and Twix pieces are being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Lowfat Yogurt with Toppers. Two-product package. Contains 8-6oz (170g) cups of Vanilla Yogurt with Snickers pieces (cup UPC 46675-00112), and 8-6oz (170g) cups of Vanilla Yogurt with Twix bar pieces (cup UPC 46675-00113). Two-Pack UPC 46675-02614. Keep Refrigerat
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0304-2025·2025-07-23

    YoCrunch strawberry and raspberry granola yogurt may contain plastic pieces

    A YoCrunch Lowfat Yogurt with Toppers two-product package containing strawberry and raspberry yogurt with granola is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Lowfat Yogurt with Toppers Two-product package. Contains 8-6oz (170g) cups of Strawberry Yogurt with Granola pieces (Cup UPC 46675-00010), and 8-6oz (170g) cups of Raspberry Yogurt with Granola pieces (Cup UPC 46675-01401). Two- Pack, UPC 46675-01401. Keep Refrige
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0291-2025·2025-07-23

    Savagely Sour blue raspberry bars recalled over potential Listeria contamination

    Savagely Sour BlueRasberry Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Savagely Sour BlueRasberry Bar (86265), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Drugs)·D-0518-2025·2025-07-23

    Levothyroxine sodium 25 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 25 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 82,159 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0288-2025·2025-07-23

    Orange Cream bars recalled over potential Listeria monocytogenes contamination

    Orange Cream Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Orange Cream Bar (86010), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·H-0298-2025·2025-07-23

    YoCrunch vanilla cookie dough yogurt multipacks may contain plastic pieces

    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Chocolate Chip Cookie Dough pieces multipacks, is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Chocolate Chip Cookie Dough pieces, Multipack containing 4-4 oz. (113g) cups. UPC 46675-01315. Keep Refrigerated. Distributed by Danone US, LLC, White Plains, NY 10605
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2115-2025·2025-07-23

    Access Vitamin B12 reagent lot can give erroneously low or high results

    Access Vitamin B12 Reagent lot 439850 is being recalled after complaints of erroneous results, which may lead to a delayed or improper diagnosis or repeat testing. 10,000 units are affected.

    Product
    Access Vitamin B12 Reagent, Catalog Number 33000, Lot Number 439850
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·H-0293-2025·2025-07-23

    Cool Watermelon bars recalled over potential Listeria monocytogenes contamination

    Cool Watermelon Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Cool Watermelon Bar (86270), stick novelties 2.5 FL. Oz (74mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·H-0296-2025·2025-07-23

    YoCrunch vanilla yogurt with Snickers pieces may contain plastic pieces

    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Snickers pieces, is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Snickers pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00112 2. Multipack containing 4-4 oz. cups UPC 46675-01326 Keep Refrigerated. Distributed by Danone US, LLC, White Pla
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0300-2025·2025-07-23

    YoCrunch strawberry yogurt with M&M toppers may contain plastic pieces

    YoCrunch Low Fat Yogurt with Toppers, Strawberry with milk chocolate M&Ms minis, is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Low Fat Yogurt with Toppers, Strawberry with milk chocolate M&Ms minis candies, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00083 2. Multipack containing 4-4 oz. cups UPC 46675-01312 Keep Refrigerated. Distributed by Dano
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0297-2025·2025-07-23

    YoCrunch vanilla yogurt with Twix pieces may contain plastic pieces

    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Twix bar pieces, is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Low Fat Yogurt with Toppers, Vanilla with Twix bar pieces, Packaged in the following size containers: 1. Single Serve Cup, 6 oz. (170g) UPC 46675-00113 2. Multipack containing 4-4 oz. cups UPC 46675-01327 Keep Refrigerated. Distributed by Danone US, LLC, White Plai
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2116-2025·2025-07-23

    SwabCap disinfecting caps may have an incomplete seal allowing alcohol evaporation

    SwabCap Disinfecting Caps for needlefree connectors are being recalled because an incomplete seal may let isopropyl alcohol evaporate, which may result in inadequate disinfection. 1,445,600 units affected.

    Product
    SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve, REF: SCXT3-5-2000; SwabCap, 200-ct. Box, REF: SCXT3-2000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0279-2025·2025-07-23

    Wei-Chuan dried black fungus slices tested positive for Salmonella

    Wei-Chuan branded Black Fungus Slice in 2.5 oz bags is being recalled because the wood-ear mushroom tested positive for Salmonella. 100 cases are affected.

    Product
    Wei-Chuan branded Black Fungus Slice. Net weight: 2.5 oz UPC#: 072869231321
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·H-0299-2025·2025-07-23

    YoCrunch strawberry granola yogurt cups may contain plastic foreign material

    YoCrunch Low Fat Yogurt with Toppers, Strawberry with Granola pieces in 6 oz single serve cups, is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Low Fat Yogurt with Toppers, Strawberry with Granola pieces, Single Serve Cup, 6 oz. (170g) UPC 46675-00010. Keep Refrigerated. Distributed by Danone US, LLC, White Plains, NY 10605
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0521-2025·2025-07-23

    Levothyroxine sodium 100 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 100 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 9,739 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2111-2025·2025-07-23

    BLS DIODE laser projectors shipped without a working remote interlock connector

    BLS laser light show projectors, models DIODE 1000, 2000 and 3000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 10 units affected.

    Product
    Laser light show projectors manufactured by BLS, Model DIODE 1000/2000/3000.
    Category
    Other
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0519-2025·2025-07-23

    Levothyroxine sodium 25 microgram bottles of 1000 assayed below specification

    Levothyroxine Sodium Tablets, USP 25 mcg in 1000-count bottles from Accord Healthcare are being recalled because the product is subpotent. 2,352 bottles are affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0525-2025·2025-07-23

    Omeprazole capsule bottle contained a foreign divalproex sodium tablet

    Omeprazole Delayed-release Capsules USP 20 mg are being recalled because a foreign Divalproex Sodium Extended-Release 250 mg tablet was found in a bottle. 1,476 bottles affected.

    Product
    OMEPRAZOLE — OMEPRAZOLE (OMEPRAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2118-2025·2025-07-23

    NIO-A intraosseous device stabilizer may not release properly after insertion

    The NIO-A NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 7,056 US units affected.

    Product
    Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000603 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intra-osseous access device supplied Sterile and single use. Indicated for Intra-osseous access t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2119-2025·2025-07-23

    NIO+ intraosseous device stabilizer may not release properly after insertion

    The NIO Intraosseous Device Adult is being recalled because a manufacturing error means the built-in stabilizer may not be released properly after deployment and insertion. 516 US units affected.

    Product
    Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000908 Software Version: N/A Product Description: NIO devices are a spring-based, automatic intraosseous access device supplied Sterile and single use. Indicated for Intraosseous access to t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0272-2025·2025-07-23

    J. Higgs potato chip mix recalled over undeclared milk allergen

    J. Higgs Potato Chip Mix, 18 one-ounce singles per bag, is being recalled because of undeclared milk. 2,275 bags are affected.

    Product
    J. Higgs Potato Chip Mix, 18 1oz singles, net weight 180z., UPC 0-51933-37327-3
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2120-2025·2025-07-23

    VITROS Performance Verifier I lots can cause quality control drift

    VITROS Chemistry Products Performance Verifier I is being recalled because quality control drift can occur with certain cholinesterase slide lots, which could produce erroneous patient results.

    Product
    Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products Performance Verifier I Model/Catalog Number: 806 7324 Software Version: Not Applicable Product Description: VITROS Chemistry Products Performance Verifier is an assayed control used to monitor perfo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0534-2025·2025-07-23

    Rizatriptan 10 mg tablets exceed the acceptable intake limit for nitrosamine

    Rizatriptan Benzoate Tablets USP 10 mg are being recalled after detection of N-nitroso-dimethyl-rizatriptan above the FDA recommended acceptable intake limit.

    Product
    RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0294-2025·2025-07-23

    YoCrunch vanilla yogurt with M&M toppers may contain plastic pieces

    YoCrunch Lowfat Yogurt with Toppers, Vanilla with milk chocolate M&Ms, is being recalled because of foreign material in the form of plastic pieces.

    Product
    YoCrunch Lowfat Yogurt with Toppers, Vanilla with milk chocolate M&Ms, Packaged in the following size containers: 1. Single Serve Cup 6 oz (170g) UPC 46675-00079 2. Multipack consisting of 4-4 oz. cups UPC 46675-01351 Keep Refrigerated. Distributed by Danone US, White Plai
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2125-2025·2025-07-23

    EMPOWR 3D knee 10mm tibial inserts were packaged with wrong implant

    EMPOWR 3D Knee Tibial Insert E-PLUS units, catalog number 341-10-711, are being recalled because of a packaging discrepancy in which incorrect tibial inserts were packaged. 20 units affected.

    Product
    Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Name: EMPOWR 3D KNEETM INS, 11L 10MM, VE Model/Catalog Number: 341-10-711 Software Version: NA Product Description: Enovis" knee devices are intended for treatment of patients who are candidates for knee arthroplasty p
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Drugs)·D-0533-2025·2025-07-23

    Rizatriptan 5 mg tablets exceed the acceptable intake limit for nitrosamine

    Rizatriptan Benzoate Tablets USP 5 mg are being recalled after detection of N-nitroso-dimethyl-rizatriptan above the FDA recommended acceptable intake limit.

    Product
    RIZATRIPTAN BENZOATE — RIZATRIPTAN BENZOATE (RIZATRIPTAN BENZOATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2122-2025·2025-07-23

    VITROS CHE slides can cause quality control drift with performance verifiers

    VITROS Chemistry Products CHE Slides are being recalled because quality control drift can occur with certain Performance Verifier lots, which could produce erroneous patient results.

    Product
    VITROS Chemistry Products CHE Slides; Catalog Numbers: (1) 191 4605 (300 slides), (2) 800 4707 (90 slides);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0520-2025·2025-07-23

    Levothyroxine sodium 50 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 50 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 54,227 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2113-2025·2025-07-23

    BLS PURE laser projectors shipped without a working remote interlock connector

    BLS laser light show projectors, models PURE 5000 and PURE 10000, are being recalled because the remote interlock connector required by federal regulation was not installed or was not wired. 3 units affected.

    Product
    Laser light show projectors manufactured by BLS, Model PURE 5000/10000.
    Category
    Other
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0524-2025·2025-07-23

    Levothyroxine sodium 175 microgram tablets assayed below the approved specification

    Levothyroxine Sodium Tablets, USP 175 mcg from Accord Healthcare are being recalled because the product is subpotent, with an assay below the approved specification. 2,344 bottles affected.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0284-2025·2025-07-23

    Chocolate crunch cake bars recalled over potential Listeria monocytogenes contamination

    Chocolate Crunch Cake Bar frozen stick novelties are being recalled because of potential Listeria monocytogenes contamination. The action covers 110,292 cases across all affected products.

    Product
    Chocolate Crunch Cake Bar (85000), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.
    Category
    Food
    Distribution
    23 states
  • ModerateFDA (Drugs)·D-0548-2025·2025-07-23

    Power Stick for her roll-on antiperspirant recalled over manufacturing deviations

    Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent is being recalled because of CGMP deviations. 21,265 cases are affected.

    Product
    Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-038-00, UPC Code 815195019313
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0549-2025·2025-07-23

    Power Stick Spring Fresh roll-on antiperspirant recalled over manufacturing deviations

    Beauty & Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant Spring Fresh is being recalled because of CGMP deviations. 22,482 cases are affected.

    Product
    Beauty & Skincare Power Stick original nourishing invisible protection roll-on Antiperspirant/Deodorant Spring Fresh, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-039-00, UPC Code 815195018194
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2114-2025·2025-07-23

    NeuroSync EYE-SYNC headsets are inoperable and cannot be repaired

    NeuroSync EYE-SYNC systems containing Pico Neo 2 headsets are being recalled because eye syncing issues render the device inoperable and it cannot be repaired. 27 units are affected.

    Product
    NeuroSync EYE-SYNC containing Pico Neo 2 Headsets. Each unit consists of a Pico Neo 2 headset with embedded sensors, a paired Android tablet, and proprietary software, packaged in a portable field case. Eye-tracking headset system is intended for recording, viewing, and analyz
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0516-2025·2025-07-23

    Lisdexamfetamine 60 mg capsules failed dissolution testing at nine month stability

    Lisdexamfetamine Dimesylate Capsules 60 mg are being recalled because an out of specification result was observed in dissolution testing at the nine month long term stability station. 5,448 bottles affected.

    Product
    LISDEXAMFETAMINE DIMESYLATE — LISDEXAMFETAMINE DIMESYLATE (LISDEXAMFETAMINE DIMESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0530-2025·2025-07-23

    Compounded parenteral nutrition bags recalled over insufficiently documented cleaning step

    Two bags of compounded Peripheral Parenteral Nutrition are being recalled because a daily cleaning step in the ISO-5 compounding area was not sufficiently documented.

    Product
    PERIPHERAL PARENTERAL NUTRITION, Compounded Sterile Preparation, Refrigerated Injection, Rx Only, Single Dose Injection, a) 1440 mL bag, b) 1700 mL bag, Central Admixture Pharmacy Services, Inc, Los Angeles, 13128 Imperial Hwy, Santa Fe Spr., CA 90870.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2127-2025·2025-07-23

    Medtronic SmartSync software update removes an erroneous electrical reset message

    Medtronic SmartLink Software on the SmartSync Patient Connector is being updated because the system could display an erroneous electrical reset message on interrogation when no reset had occurred. 3,909 units affected.

    Product
    Medtronic SmartLink Software loaded on SmartSync Patient Connector, Model Number 24967 with the following software components: 1. Azure Astra application, Software Model Number D00U003; 2. Percepta Serena Solara application, Software Model Number D00U004; 3. Cobalt Crome
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·H-0280-2025·2025-07-23

    Pasteurized donor human milk bottles have plastic particulate under the cap

    Pasteurized Donor Human Milk in 4 oz bottles is being recalled because plastic particulate from the outer closure was found between the foil seal and the plastic cap. 209 bottles are affected.

    Product
    Pasteurized Donor Human Milk , 4oz plastic bottle
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0273-2025·2025-07-23

    New Mexico Pinon single serve coffee cup ink can run

    New Mexico Pinon Coffee Dark Pinon Single Serve cups are being recalled because an inconsistent clear coat seal allows the food safe ink printing to run in a K-cup machine. 154 units affected.

    Product
    New Mexico Pinon Coffee. Dark Pinon Single Serve 10ct. Product Number:F03308 UPC:812361033081. Single Serve (Keurig) Cups, filled with ground coffee flavored with natural flavorings.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0321-2025·2025-07-23

    Boar's Head smoked gouda recalled in Florida over product mislabeling

    Boar's Head Smoked Gouda in 8 oz packages is being recalled because of mislabeling. 65 cases are affected, distributed in Florida.

    Product
    Boar's Head Smoked Gouda, Net Wt 8 oz (226g). UPC 0 42421-50006 6. Keep Refrigerated. Distributed by Brunckhorst Co., NY,NY 11206.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2124-2025·2025-07-23

    Culture media quality control kits contain the wrong bacterial organism

    KWIK-STIK and LYFO DISK quality control kits for culture media are being recalled because affected products contain Staphylococcus epidermidis instead of the expected Brevundimonas diminuta. 21 units affected.

    Product
    KWIK-STIK and LYFO DISK, quality control kit for culture media Catalog # 0805K and 0805L
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0550-2025·2025-07-23

    Power Stick roll-on antiperspirant recalled over manufacturing practice deviations

    Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant is being recalled because of CGMP deviations. 23,467 cases are affected.

    Product
    Shave and Skincare Power Stick Original Nourishing Invisible Protection Roll-On Antiperspirant/Deodorant, 1.8 oz./ 53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-040-00 UPC Code 815195018224
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2128-2025·2025-07-23

    Medtronic CareLink SmartSync software update removes an erroneous reset message

    Medtronic SmartLink software on the CareLink SmartSync Device Manager is being updated because the system could display an erroneous electrical reset message on interrogation when no reset had occurred. 5,418 units affected.

    Product
    Medtronic SmartLink software loaded on CareLink SmartSync Device Manager, Model Number 24967A with the following software components: 1. Azure Astra application, Software Model Number D00U003; 2. Percepta Serena Solara application, Software Model Number D00U004; 3. Cobal
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Drugs)·D-0517-2025·2025-07-23

    Compounded testosterone pellet vials carry incorrect lot numbers from printing issue

    Compounded Testosterone 200 mg Pellet in 1 mL amber vials is being recalled because a printing issue resulted in incorrect lot numbers on the label. 2,832 vials are affected.

    Product
    Testosterone 200 mg Pellet packaged in 1mL amber vials, Rx only, Compounded product. Qualgen 14844 Bristol Park Blvd Edmond OK 73013, NDC 69761-202-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V478000·2025-07-22

    Winnebago airbag wiring can be caught in the seat mechanism

    Winnebago is recalling certain 2024-2026 motorhomes because Supplemental Restraint System wires can be caught in the seat mechanism when the front seats are adjusted, damaging them.

    Product
    WINNEBAGO — WINNEBAGO EKKO, NAVION, VIEW, REVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V476000·2025-07-22

    Nova Bus steering can turn without driver input from missing valve

    Nova Bus is recalling certain 2020-2023 LFS transit buses because the electric power steering system may be missing a check valve, allowing hydraulic pressure to turn the steering wheel on its own.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide

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